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A 10 bp Deletion Polymorphism and 2 New Variations in the GLUT1 Gene Associated With Meningomyelocele

We sought to examine the diversity and extent of sequence variations in GLUT1 in patients with myelomeningocele (MM) and to identify variations conferring risk of MM. Sequences of the 10 exons and exon-intron boundaries of GLUT1 for 96 patients with MM (48 Caucasians and 48 Mexican Americans) were d...

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Autors principals: Cormier, Clint M., Au, Kit Sing, Northrup, Hope
Format: Artigo
Idioma:Inglês
Publicat: SAGE Publications 2011
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3117222/
https://ncbi.nlm.nih.gov/pubmed/21135204
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1933719110388293
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